{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "Software error VE10B -In case of a fault within the drivetrain of an axis and while performing a stepped peripheral imaging (PERISTEPPING/PERIVISION), the C-arm may leave its intended travel path by up to 22 cm (9\") result in canceling clinical treatment or to continue treatment on an alternative system",
      "address_2": "",
      "product_quantity": "116 units",
      "code_info": "Software VE10B.  Serial Numbers:  164138  164159  164033  164287  164282  164210  164183  164184  164311  164142  164071  164328  164034  164318  164244  164242  164306  164155  164189  164271  164277  164173  164292  164231  164057  164054  164055  164080  164132  164329  164072  164088  164190  164333  164025  164026  164027  164338  164094  164241  164326  164267  164186  164068  164121  164157  164019  164152  164161  164013  164069  164213  164073  164257  164293  164263  164298  164060  164083  164113  164021  164066  164124  164125  164279  164075  164074  164084  164086  164098  164028  164153  164330  164295  164234  164321  164270  164275  164315  164163  164158  164053  164171  164134  164253  164188  164063  164064  164299  164300  164105  164160  164024  164049  164240  164227  164228  164018  164022  164250  164061  164187  164115  164322  164269  164303  164204  164205  164211  164212  164216  164196  164168  164319  164201  164202",
      "center_classification_date": "20210707",
      "distribution_pattern": "US Nationwide",
      "state": "PA",
      "product_description": "ARTIS pheno- angiography systems developed for single and biplane diagnostic imaging and interventional procedures.  Model:   10849000",
      "report_date": "20210714",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-2029-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "88216",
      "more_code_info": "",
      "recall_initiation_date": "20210527",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}